terbinafine

Generic: terbinafine

Labeler: exelan pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name terbinafine
Generic Name terbinafine
Labeler exelan pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

terbinafine hydrochloride 250 mg/1

Manufacturer
Exelan Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 76282-209
Product ID 76282-209_dc86cdd6-0a8a-4e5c-b3c4-8b05388af862
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077533
Listing Expiration 2026-12-31
Marketing Start 2012-04-25

Pharmacologic Class

Classes
allylamine antifungal [epc] allylamine [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 76282209
Hyphenated Format 76282-209

Supplemental Identifiers

RxCUI
313222
UPC
0376282209302
UNII
012C11ZU6G

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name terbinafine (source: ndc)
Generic Name terbinafine (source: ndc)
Application Number ANDA077533 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (76282-209-01)
  • 500 TABLET in 1 BOTTLE (76282-209-05)
  • 30 TABLET in 1 BOTTLE (76282-209-30)
source: ndc

Packages (3)

76282-209-01 100 TABLET in 1 BOTTLE (76282-209-01) 76282-209-05 500 TABLET in 1 BOTTLE (76282-209-05) 76282-209-30 30 TABLET in 1 BOTTLE (76282-209-30)

Ingredients (1)

terbinafine hydrochloride (250 mg/1)

Linked Drug Pages (1)

Terbinafine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "dc86cdd6-0a8a-4e5c-b3c4-8b05388af862", "openfda": {"upc": ["0376282209302"], "unii": ["012C11ZU6G"], "rxcui": ["313222"], "spl_set_id": ["6dc279cc-9861-4fa8-8083-ca3b3c57b513"], "manufacturer_name": ["Exelan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (76282-209-01)", "package_ndc": "76282-209-01", "marketing_start_date": "20120425"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (76282-209-05)", "package_ndc": "76282-209-05", "marketing_start_date": "20120425"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (76282-209-30)", "package_ndc": "76282-209-30", "marketing_start_date": "20120425"}], "brand_name": "Terbinafine", "product_id": "76282-209_dc86cdd6-0a8a-4e5c-b3c4-8b05388af862", "dosage_form": "TABLET", "pharm_class": ["Allylamine Antifungal [EPC]", "Allylamine [CS]"], "product_ndc": "76282-209", "generic_name": "Terbinafine", "labeler_name": "Exelan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Terbinafine", "active_ingredients": [{"name": "TERBINAFINE HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "ANDA077533", "marketing_category": "ANDA", "marketing_start_date": "20120425", "listing_expiration_date": "20261231"}